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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543358Generated: November 3, 2026

Chlorotrimethylsilane → Trimethylsilyl dibutylphosphinite

https://huagongshe.com/reaction/543358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiethylphosphiteHCID 3780918—
ReactantHCID 178418682HCID 178418682—
ReactantHCID 178454905HCID 178454905—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
ProductTrimethylsilyl dibutylphosphiniteHCID 1265138986%

Reaction Conditions

Temperature80 °C

Reaction Steps

The procedure described in Tetrahedron, 1967, 23, 1065 (M. Grayson et al.) was followed. Dibutylphosphine oxide, prepared from butyl magnesium bromide and diethylphosphite, (3.3 g, 20 mmol) and triethylamine (2.02 g, 20 mml) were dissolved in toluene (20 mL) and treated with a solution of trimethylsilyl chloride (2.17 g, 20 mmol) in toluene (5 mL) at room temperature. The solution got very warm and a precipitate formed immediately. The mixture was heated at 80° C. for two hours, then filtered, washed with toluene, and concentrated. Kugelrohr distillation at 80° C. (1.5 mmHg) afforded 4.1 g (86%) of the desired product. 1H NMR (CDCl3) δ1.8-1.2 (m, 6H), 1.1-0.7 (m, 3H), 0.17 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661615
Source datasetuspto-grants-1987_04
ORD IDord-2725d2c25fb2441e9da8c274f3f419fa
Source noteuspto-grants-1987_04